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Gait disorders/ataxia
Citations 141-144 of 144 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1
- Y. Miyoshi, T. Yamada, M. Tanimura, T. Taniwaki, K. Arakawa, Y. Ohyagi, H. Furuya, K. Yamamoto, K. Sakai, T. Sasazuki, and J. Kira
Neurology 2001; 57: 96-100.
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- CLINICAL/SCIENTIFIC NOTES
Serum transferrin receptor levels in Friedreich’s and other degenerative ataxias
- V. Scarano, T. de Cristofaro, G. De Michele, E. Salvatore, I. De Biase, A. Monticelli, A. Filla, and S. Cocozza
Neurology 2001; 57: 159-160.
[Abstract]
[Full text]
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- ARTICLES
Clinical features and genetic analysis of a new form of spinocerebellar ataxia
- D. Devos, S. Schraen–Maschke, I. Vuillaume, K. Dujardin, P. Nazé, C. Willoteaux, A. Destée, and B. Sablonnière
Neurology 2001; 56: 234-238.
[Abstract]
[Full text]
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- ARTICLES
Relationship of substantia nigra echogenicity and motor function in elderly subjects
- Daniela Berg, Christiane Siefker, Petra Ruprecht-Dörfler, and Georg Becker
Neurology 2001; 56: 13-17.
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